Cryo Global Registry

Status Active, not recruiting

Clinical Trial Summary

Cryo Global Registry a prospective, global, multi-center, observational Post-Market Registry

Clinical Trial Description

The Cryo Global Registry is a prospective, global, multi-center, observational post-market registry (PMR). The purpose of this study is to evaluate and describe clinical performance and safety data in a broad patient population treated with a commercially available Arctic Front™ Family of Cardiac Cryoablation Catheters (hereafter referred to as "Arctic Front™ Cardiac Cryoablation Catheter System"). The cryoballoon ablation(CBA) procedure will be performed according to routine hospital practice. The study is expected to have a 24 month enrollment period. The follow up period is intended to align with standard practice and subjects will be followed for a minimum of 12 months post-procedure. ;

Study Design

Related Conditions & MeSH terms

Atrial Fibrillation

Clinical Trial Details

NCT number	NCT02752737
Study type	Observational [Patient Registry]
Source	Medtronic Cardiac Rhythm and Heart Failure
Contact
Status	Active, not recruiting
Phase
Start date	May 2016
Completion date	January 2028

View Details

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